Canonical Allele Identifier: CA2735778069
Gene: NFIX HGNC NCBI

Linked Data

dbSNP Id: rs2145475371

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13081691del , CM000681.2:g.13081691del GRCh38
NC_000019.9:g.13192505del , CM000681.1:g.13192505del GRCh37
NC_000019.8:g.13053505del NCBI36
NG_032925.2:g.90922del

Transcript Alleles

HGVS Amino-acid change
ENST00000358552.8:c.964del ENSP00000351354.5:p.Ala322ProfsTer?
ENST00000622520.2:c.1075+2956del ENSP00000481181.2:n.1075+2956del
ENST00000693124.1:c.773+6020del
ENST00000592199.6:c.1090del MANE Select ENSP00000467512.1:p.Ala364ProfsTer?
ENST00000676441.1:c.1114del ENSP00000502554.1:p.Ala372ProfsTer?
ENST00000358552.7:c.976del ENSP00000351354.4:p.Ala326ProfsTer?
ENST00000360105.8:c.976del ENSP00000353219.4:p.Ala326ProfsTer?
ENST00000397661.6:c.1090del ENSP00000380781.2:p.Ala364ProfsTer?
ENST00000585382.5:c.*459del ENSP00000466605.1:n.*459del
ENST00000585575.5:c.1066del ENSP00000468794.1:p.Ala356ProfsTer?
ENST00000586797.5:c.*921del ENSP00000467536.1:n.*921del
ENST00000587260.1:c.1087del ENSP00000467785.1:p.Ala363ProfsTer?
ENST00000587760.5:c.1066del ENSP00000466389.1:p.Ala356ProfsTer?
ENST00000588228.5:c.949del ENSP00000466735.1:p.Ala317ProfsTer?
ENST00000592199.5:c.1090del ENSP00000467512.1:p.Ala364ProfsTer?
NM_001271043.2:c.1114del NP_001257972.1:p.Ala372ProfsTer?
NM_001271044.2:c.1066del NP_001257973.1:p.Ala356ProfsTer?
NM_002501.3:c.1090del NP_002492.2:p.Ala364ProfsTer?
XM_005259917.3:c.1144del XP_005259974.1:p.Ala382ProfsTer?
XM_005259918.3:c.1090del XP_005259975.1:p.Ala364ProfsTer?
XM_005259919.3:c.1267del XP_005259976.1:p.Ala423ProfsTer?
XM_005259920.3:c.1066del XP_005259977.1:p.Ala356ProfsTer?
XM_005259921.3:c.1255+2956del XP_005259978.1:n.1255+2956del
XM_005259922.3:c.1132+6020del XP_005259979.1:n.1132+6020del
XM_006722760.2:c.1144del XP_006722823.1:p.Ala382ProfsTer?
XM_011528040.1:c.1138del XP_011526342.1:p.Ala380ProfsTer?
NM_001365902.1:c.1090del NP_001352831.1:p.Ala364ProfsTer?
NM_001365982.1:c.967del NP_001352911.1:p.Ala323ProfsTer?
NM_001365983.1:c.949del NP_001352912.1:p.Ala317ProfsTer?
NM_001365984.1:c.1087del NP_001352913.1:p.Ala363ProfsTer?
NM_001365985.1:c.1087del NP_001352914.1:p.Ala363ProfsTer?
XM_005259917.4:c.1144del XP_005259974.1:p.Ala382ProfsTer?
NM_001271044.3:c.1066del NP_001257973.1:p.Ala356ProfsTer?
NM_001365902.2:c.1090del NP_001352831.1:p.Ala364ProfsTer?
NM_001365982.2:c.967del NP_001352911.1:p.Ala323ProfsTer?
NM_001365983.2:c.949del NP_001352912.1:p.Ala317ProfsTer?
NM_001365984.2:c.1087del NP_001352913.1:p.Ala363ProfsTer?
NM_001365985.2:c.1087del NP_001352914.1:p.Ala363ProfsTer?
NM_002501.4:c.1090del NP_002492.2:p.Ala364ProfsTer?
NM_001365902.3:c.1090del MANE Select NP_001352831.1:p.Ala364ProfsTer?
NM_001378404.1:c.1066del NP_001365333.1:p.Ala356ProfsTer?
NM_001378405.1:c.1138del NP_001365334.1:p.Ala380ProfsTer?